Related Experiment Video
Updated: Jul 11, 2025

Evaluation of Drug Sorption to PVC- and Non-PVC-based Tubes in Administration Sets Using a Pump
Published on: March 11, 2017
Solid solution polymorphs afford two highly soluble co-drug forms of tolbutamide and chlorpropamide
Enrico Spoletti1, Vivek Verma1, Chiara Cappuccino1
1Department of Chemical Science and Bernal Institute, University of Limerick, Limerick, V94 T9PX, Ireland. matteo.lusi@ul.ie.
Abstract:
The search for solid solutions of class-two insulin secretagogues, tolbutamide and chlorpropamide, reveals a rare case of monotropic polymorphism for the mixed crystals. At any stoichiometry, two crystal forms are isolated that are kinetically stable at room temperature from a few months to over a year. Dissolution tests certify the solubility advantage of the solid solutions over the pure drugs as well as their physical mixture, suggesting a potential application as a highly soluble co-drug formulation.
Related Concept Videos
Factors Affecting Dissolution: Polymorphism, Amorphism and Pseudopolymorphism
Some polymorphic crystals possess lower aqueous solubility than their amorphous counterparts, leading to incomplete absorption. For instance, the oral suspension of Chloramphenicol, which...
Drug Biotransformation: Overview
Drug Distribution: Tissue Binding
For...
Drug-Receptor Bonds
In...
Drug Metabolism: Phase II Reactions
Pore Transport and Ion-Pair Transport
Pore transport, also known as convective transport, is a process where small molecules like urea, water, and sugars rapidly cross cell membranes as though there were channels or pores in the membrane. Although direct microscopic evidence is limited but the concept of pores or channels is widely accepted based on physiological evidence. Despite the lack of direct...

